Phenotype #0000262577

Individual ID 00367239
Associated disease -
Phenotype details At the age of 22, the BCVA (RE) was 0,05 and the BCVA (LE) was 0,05. At the age of 22 the fundus showed: Macular atrophy. Widespread flecks over the posterior pole, peripapillary sparing.
Diagnosis/Initial Stargardt disease
Inheritance Unknown
Diagnosis/Definite STGD1
Age/Examination -
Age/Diagnosis -
Age/Onset 16y
Phenotype/Onset unknown
Protein -
Owner name Stéphanie Cornelis
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Stéphanie Cornelis
Date created 2021-05-03 14:25:36 +02:00 (CEST)
Date last edited N/A

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